Agenesis of Corpus Callosum

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  Subject Areas on Research

  • Abnormalities in MRI-measured signal intensity in the corpus callosum in schizophrenia. 
  • Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome. 
  • Brain malformation and infantile spasms in a SCAD deficiency patient. 
  • Concurrent agenesis of the corpus callosum and ureteroceles in siblings. 
  • Facilitation of infantile spasms by partial seizures. 
  • Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series. 
  • Malposition of the attached portion of the falx cerebri and the superior sagittal sinus. An indicator of severe cerebral maldevelopment. 
  • Pyridoxine-dependent seizures and cognition in adulthood. 
  • Septo-optic dysplasia with olfactory tract and bulb hypoplasia. 
  • The effect of corpus callosum agenesis on neocortical thickness and neuronal density of BALB/cCF mice. 
  • Third ventricle: size and appearance in normal fetuses through gestation.